Estetrol-d4 (Major)

CAS : 15183-37-6

Ref. TR-E668452

Informations sur le produit

• Nom: Estetrol-d4 (Major)
• Synonymes: (15a,16a,17ß)-Estra-1,3,5(10)-triene-3,15,16,17-tetrol-d4, Estra-1,3,5(10)-triene-3,15a,16a,17ß-tetrol-d4, 15a-Hydroxyestriol-d4, 3,15a,16a,17ß-Tetrahydroxyestra-1,3,5(10)-triene-d4, (15Alpha,16Alpha,17Beta)-Estra-1,3,5(10)-Triene-3,15,16,17-Tetrol, (15a,16a,17)-Estra-1,3,5(10)-triene-3,15,16,17-tetrol, (15α,16α,17β)-Estra-1,3,5(10)-triene-3,15,16,17-tetrol, 1,3,5(10)-Estratrien-3,15-Alpha, 16-Alpha, 17-Beta-Tetrol, 15-Alpha-Hydroxyestriol, 15a-Hydroxyestriol, 3,15a,16a,17-Tetrahydroxyestra-1,3,5(10)-triene, 3,15α,16α,17β-Tetrahydroxyestra-1,3,5(10)-triene, E 4, Enb 39R14Vf, Estra-1,3,5(10)-trien-3,15α,16α,17β-tetraol, Estra-1,3,5(10)-triene-3,15,16,17-tetrol, (15α,16α,17β)-, Estra-1,3,5(10)-triene-3,15a,16a,17-tetrol, Estra-1,3,5(10)-triene-3,15α,16α,17β-tetrol, Estetrol

Description

Applications A labelled metabolite of Estradiol. It is an estrogenic steroid synthesized exclusively by the fetal liver during human pregnancy and reaching the maternal circulation through the placenta.
References Gurpide, E., et al.: J. Clin. Endocrinol., 26, 1355 (1966), Hagen, A., et al.: J. Clin. Endocrinol., 30, 763 (1970), Schollberg, K., et al.: Exp. Clin. Endocrinol., 85, 204 (1985), Coelingh Bennink, H., et al.: Contraception, 77, 186 (2008),

• Marque: TRC

Propriétés chimiques

• Masse moléculaire: 308.41
• Formule: C₁₈H₂₀D₄O₄
• Couleur/Forme: White To Off-White
• InChI: InChI=1S/C18H24O4/c1-18-7-6-12-11-5-3-10(19)8-9(11)2-4-13(12)14(18)15(20)16(21)17(18)22/h3,5,8,12-17,19-22H,2,4,6-7H2,1H3/t12-,13-,14-,15-,16-,17+,18+/m1/s1/i2D2,3D,8D
• Code InChI: InChIKey=AJIPIJNNOJSSQC-SCCHASIWSA-N
• SMILES: [2H]c1cc2c(c([2H])c1O)C([2H])([2H])C[C@@H]1[C@@H]2CC[C@@]2(C)[C@H]1[C@@H](O)[C@@H](O)[C@@H]2O